Canonical Allele Identifier: CA2026936852

Gene: ALG10

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.34026832G= , CM000674.2:g.34026832G=	GRCh38
NC_000012.11:g.34179767G= , CM000674.1:g.34179767G=	GRCh37
NC_000012.10:g.34071034G=	NCBI36
NG_016389.1:g.9552G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266483.7:c.1339G= MANE Select	ENSP00000266483.2:p.Val447=
ENST00000266483.6:c.1339G=	ENSP00000266483.2:p.Val447=
ENST00000538927.1:c.369+2673G=	ENSP00000444084.1:n.369+2673G=
ENST00000541875.1:c.*1079G=	ENSP00000443142.1:n.*1079G=
NM_032834.3:c.1339G=	NP_116223.3:p.Val447=
XM_024449230.1:c.1159G=	XP_024304998.1:p.Val387=
XM_024449231.1:c.1159G=	XP_024304999.1:p.Val387=
NM_032834.4:c.1339G= MANE Select	NP_116223.3:p.Val447=